APA (7th ed.) Citation

Hae In Lee, Ahreum Kwon, Jung Hwan Suh, Han Saem Choi, Kyung Chul Song, Hyun Wook Chae, & Ho-Seong Kim. (2021). Two cases of 17α-hydroxylase/17,20-lyase deficiency caused by the CYP17A1 mutation. Korean Society of Pediatric Endocrinology.

Chicago Style (17th ed.) Citation

Hae In Lee, Ahreum Kwon, Jung Hwan Suh, Han Saem Choi, Kyung Chul Song, Hyun Wook Chae, and Ho-Seong Kim. Two Cases of 17α-hydroxylase/17,20-lyase Deficiency Caused by the CYP17A1 Mutation. Korean Society of Pediatric Endocrinology, 2021.

MLA (9th ed.) Citation

Hae In Lee, et al. Two Cases of 17α-hydroxylase/17,20-lyase Deficiency Caused by the CYP17A1 Mutation. Korean Society of Pediatric Endocrinology, 2021.